The Rush Alzheimer?s Disease Core Center (Rush ADCC; P30AG10161) supports cutting edge and innovative research on the etiology, pathogenesis, diagnosis, treatment, and prevention of mild cognitive impairment (MCI), Alzheimer's disease (AD), and other common conditions of aging, by providing researchers with a stimulating environment, highly valued clinical and post-mortem data, and ante- and post-mortem biologic specimens. The Rush ADCC supports a variety of timely and important areas of research including risk factors for the transition from normal aging to MCI to AD, the neurobiology of normal aging and MCI, and studies that incorporate contemporary omics technologies and neuroimaging to identify novel therapeutic targets. These research areas are supported through the careful design and integration of seven highly successful Cores: an Administrative Core; Clinical Core; Data Management and Statistics Core; Neuropathology Core; Outreach, Recruitment and Education Core; Religious Orders Study Core, and Latino Core, as well as the Research Education Component. The Rush ADCC and its ancillary studies including the Rush Memory and Aging Project and the Minority Aging Research Study are building a vibrant neuroimaging portfolio of studies, some of which include participants of the Clinical and Religious Orders Study Cores for in-vivo imaging, and in collaboration with the Neuropathology Core for ex-vivo imaging. We are now generating autopsies on persons without dementia who have undergone in-vivo imaging. These are mostly non-Latino whites. Now that we have a relatively large number of African Americans and Latinos in the Clinical and Latino Cores, with a growing number of autopsies, we are in a position to expand this work in the minority communities. The overall goal of the proposed Neuroimaging Core is to generate a resource of neuroimaging data from the Rush ADCC African Americans and Latinos, and affiliated studies, and provide neuroimaging expertise to facilitate high quality, cutting edge, externally-funded research focusing on the transition from normal aging to mild cognitive impairment (MCI) to the earliest stages of Alzheimer?s disease (AD) and other dementias. The proposed Neuroimaging Core will markedly extend the ability of the Rush ADCC to interrogate neuroimaging as part of its clinical-imaging-multi-level omics-pathology pipeline supporting studies of the transition from normal aging to MCI to the earliest stages of dementia, and studies of ante- and post-mortem biospecimens, and extend this work into the African American and Latino communities which are vastly under- represented.

Public Health Relevance

The development of robust biomarkers is a major priority in AD research. The proposed Neuroimaging Core, in collaboration with the Rush ADCC ancillary studies, will generate a truly unique resource of ante-mortem imaging from African American and Latino persons with ante-mortem biofluids who come to brain autopsy without dementia. This resource will enable linking brain omics, to biofluid omics to brain pathology, neuroimaging, and cognitive and motor function in minorities to complement a similar resource of non-Latino whites that we are currently generating; we will make this resource available to the wide aging and AD research community.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
3P30AG010161-27S1
Application #
9416596
Study Section
Special Emphasis Panel (ZAG1)
Program Officer
Silverberg, Nina B
Project Start
1997-08-15
Project End
2021-06-30
Budget Start
2017-09-15
Budget End
2018-06-30
Support Year
27
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Rush University Medical Center
Department
Neurosciences
Type
Schools of Medicine
DUNS #
068610245
City
Chicago
State
IL
Country
United States
Zip Code
60612
Zhou, Zilu; Wang, Weixin; Wang, Li-San et al. (2018) Integrative DNA copy number detection and genotyping from sequencing and array-based platforms. Bioinformatics 34:2349-2355
Malek-Ahmadi, Michael; Chen, Kewei; Perez, Sylvia E et al. (2018) Cognitive composite score association with Alzheimer's disease plaque and tangle pathology. Alzheimers Res Ther 10:90
Kamara, Dennis M; Gangishetti, Umesh; Gearing, Marla et al. (2018) Cerebral Amyloid Angiopathy: Similarity in African-Americans and Caucasians with Alzheimer's Disease. J Alzheimers Dis 62:1815-1826
Ross, Ryan D; Shah, Raj C; Leurgans, Sue et al. (2018) Circulating Dkk1 and TRAIL Are Associated With Cognitive Decline in Community-Dwelling, Older Adults With Cognitive Concerns. J Gerontol A Biol Sci Med Sci 73:1688-1694
Cheng, Hao; Xuan, Hongwen; Green, Christopher D et al. (2018) Repression of human and mouse brain inflammaging transcriptome by broad gene-body histone hyperacetylation. Proc Natl Acad Sci U S A 115:7611-7616
Bennett, Rachel E; Robbins, Ashley B; Hu, Miwei et al. (2018) Tau induces blood vessel abnormalities and angiogenesis-related gene expression in P301L transgenic mice and human Alzheimer's disease. Proc Natl Acad Sci U S A 115:E1289-E1298
McAninch, Elizabeth A; Rajan, Kumar B; Evans, Denis A et al. (2018) A Common DIO2 Polymorphism and Alzheimer Disease Dementia in African and European Americans. J Clin Endocrinol Metab 103:1818-1826
Power, Melinda C; Mormino, Elizabeth; Soldan, Anja et al. (2018) Combined neuropathological pathways account for age-related risk of dementia. Ann Neurol 84:10-22
Samieri, Cécilia; Morris, Martha-Clare; Bennett, David A et al. (2018) Fish Intake, Genetic Predisposition to Alzheimer Disease, and Decline in Global Cognition and Memory in 5 Cohorts of Older Persons. Am J Epidemiol 187:933-940
Burke, Shanna L; Hu, Tianyan; Fava, Nicole M et al. (2018) Sex differences in the development of mild cognitive impairment and probable Alzheimer's disease as predicted by hippocampal volume or white matter hyperintensities. J Women Aging :1-25

Showing the most recent 10 out of 786 publications